A. van der Veen

发表

Breakpoint mapping by FISH in a Sotos patient with a constitutional translocation t(3;6)

K. Kok, C. Buys, C. Schrander‐Stumpel, 1999, Journal of medical genetics.

RFP2, c13ORF1, and FAM10A4 are the most likely tumor suppressor gene candidates for B-cell chronic lymphocytic leukemia.

E. Vellenga, M. Looman, C. Buys, 2003, Cancer genetics and cytogenetics.

Renal oncocytoma with t(5;12;11), der(1)t(1;8) and add(19): “true” oncocytoma or chromophobe adenoma?

E. van den Berg, A. Veen, E. Berg, 1997, International journal of cancer.

Normal FHIT transcripts in renal cell cancer‐ and lung cancer‐derived cell lines, including a cell line with a homozygous deletion in the FRA3B region

S. Naylor, K. Kok, C. Buys, 1997, Genes, chromosomes & cancer.

Characterization of three new variant type cell lines derived from small cell carcinoma of the lung.

L. de Leij, P. Postmus, S. Poppema, 1985, Cancer research.

Localization of amplified c-myc and n-myc in small cell lung cancer cell lines.

J. Osinga, K. Kok, C. Buys, 1989, Cancer genetics and cytogenetics.

A homozygous deletion in a small cell lung cancer cell line involving a 3p21 region with a marked instability in yeast artificial chromosomes.

K. Kok, W. V. D. Van de Ven, E. Schoenmakers, 1994, Cancer research.

Deletion of the multidrug resistance protein MRP1 gene in acute myeloid leukemia: the impact on MRP activity.

E. van den Berg, E. D. de Vries, E. Vellenga, 2000, Blood.

Localization and intron usage analysis of the human CPT1B gene for muscle type carnitine palmitoyltransferase I.

P. Terpstra, F. R. van der Leij, J. R. Kuipers, 1997, Biochimica et biophysica acta.

FISH and array‐CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions

K. Kok, C. Buys, B. Sikkema-Raddatz, 2006, American Journal of Medical Genetics. Part A.

Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)].

R. V. van Lingen, R. Sijmons, B. Leegte, 1993, American journal of medical genetics.

A gene from human chromosome region 3p21 with reduced expression in small cell lung cancer.

J. Osinga, R. Hofstra, K. Kok, 1992, Cancer research.

Infantile and adult testicular germ cell tumors. a different pathogenesis?

W. Molenaar, A. Y. van der Veen, B. de Jong, 2002, Cancer genetics and cytogenetics.

Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22.

R. V. van Lingen, R. Hofstra, C. Buys, 1999, American journal of medical genetics.

On the elucidation of a tumour suppressor role of 3p in lung cancer

M. Wei, M. Lerman, D. Angeloni, 2006 .

Effects on chromosomal proteins in sister chromatid differentiation by incorporation of 5-bromodeoxyuridine into DNA.

J. Osinga, C. Buys, A. Y. van der Veen, 1982, Experimental cell research.

Isolated metaphase chromosomes stabilized by DNA-intercalation or polyamine addition: a comparison.

J. Aten, J. Osinga, C. Buys, 1984, Cell Biology International Reports.

Follicular lymphoma grade 3B includes 3 cytogenetically defined subgroups with primary t(14;18), 3q27, or other translocations: t(14;18) and 3q27 are mutually exclusive.

E. Haralambieva, E. van den Berg, S. Poppema, 2003, Blood.

Cytogenetics of a malignant ovarian germ‐cell tumor

C. Burger, H. C. van der Linden, B. de Jong, 1998, International journal of cancer.

Allelic gains and losses in distinct regions of chromosome 6 in gastric carcinoma.

K. Kok, R. Seruca, C. Buys, 2001, Cancer genetics and cytogenetics.

Functional analysis of lung tumor suppressor activity at 3p21.3

P. Terpstra, K. Kok, F. Gerbens, 2006, Genes, chromosomes & cancer.

Two small cell lung cancer cell lines established from rigid bronchoscope biopsies.

P. Postmus, C. Buys, G. Mesander, 1988, European journal of cancer & clinical oncology.

Genome analysis of small cell lung cancer (SCLC) and clinical significance.

J. Osinga, P. Postmus, C. Buys, 1987, European journal of respiratory diseases. Supplement.

Identification of a tumor marker chromosome by flow sorting, DNA amplification in vitro, and in situ hybridization of the amplified product

J. Aten, J. Osinga, C. Buys, 1993, Genes, chromosomes & cancer.

Prenatal diagnosis in two cases of de novo complex balanced chromosomal rearrangements. Three‐year follow‐up in one case

J. R. Beekhuis, R. Sijmons, A. Veen, 1995, Prenatal diagnosis.

Two unbalanced segregation products due to a maternal t(7;16)inv(16)

R. Hordijk, B. Leegte, J. Cobben, 2001, Prenatal diagnosis.

An evolutionary rearrangement of the Xp11.3-11.23 region in 3p21.3, a region frequently deleted in a variety of cancers.

P. Terpstra, S. Naylor, K. Kok, 1999, Genomics.

Defining the position of the breakpoint of the constitutional t(3;6) occurring in a family with renal cell carcinoma

G. Kovacs, R. Gemmill, H. Drabkin, 1995, Genes, chromosomes & cancer.

Ordering of polymorphic markers in the chromosome region 3p21.

K. Kok, D. de Jong, R. Kooy, 1996, Cytogenetics and cell genetics.